Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism. [electronic resource]
Producer: 20020502Description: 1007-11 p. digitalISSN:- 0340-6245
- Adolescent
- Age of Onset
- Amino Acid Substitution
- Antithrombin III -- chemistry
- Antithrombin III Deficiency -- epidemiology
- Binding Sites
- Brain Ischemia -- genetics
- DNA Mutational Analysis
- Female
- Genetic Predisposition to Disease
- Genotype
- Humans
- Infant
- Infant, Newborn
- Infarction, Middle Cerebral Artery -- genetics
- Male
- Mutation, Missense
- Point Mutation
- Thromboembolism -- genetics
- Thrombophilia -- epidemiology
- Venous Thrombosis -- genetics
- Yugoslavia -- epidemiology
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Publication Type: Case Reports; Journal Article; Review
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